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基底细胞痣综合征是一种常染色体显性遗传性疾病,其特点是多发性基底细胞痣,多发性颌骨囊肿,骨骼系统异常,颅内异常钙化等少见的综合征,我科于1985年11月收治一例,现报道如下:患者王××,女,20岁,住院号1408045。患者因上、下颌骨多发性囊肿,曾于1980年6月23日在本科行左侧上颌骨囊肿及双侧下颌骨囊肿摘除术。病理报告为上颌骨鳞状上皮内衬之纤维囊壁组织,双侧下颌骨牙源性囊肿。一年前自觉左侧上颌略膨隆,逐渐增大,今年5月又发现右侧下颌骨膨隆,时有口腔内溢脓。诊断为颌骨多发性囊肿术后复发,于
Basal cell nevus syndrome is an autosomal dominant genetic disease characterized by multiple basal cell nevus, multiple jaw cysts, skeletal system abnormalities, intracranial abnormal calcification and other rare syndromes, our department in 1985 A case of November admitted, are reported as follows: Patient Wang × ×, female, 20 years old, hospital number 1408045. Patients due to the upper and lower jaw multiple cysts, was June 23, 1980 undergraduate on the left side of the maxillary cyst and bilateral mandibular cyst excision. The pathology was reported as the fibrous wall of the maxillary squamous epithelium and the bilateral mandibular odontogenic cyst. A year ago conscious left slightly bulging upper jaw, gradually increased in May this year and found the right mandibular bulla, sometimes with oral pus. Diagnosis of multiple recurrence of jaw cyst after surgery, in